Atlas Surgical and Prosthetic Instrumentation Kit AK-3

GUDID 07350081494872

ATLAS Surgical and Prosthetic Instrumentation kit - Drill System 2 3x CePo Drills - Short (=1.8 mm implants, 2.2, 2.4 ) - Drill System 2 1x R/A Hpc. I

Dentatus AB

Dental implant suprastructure kit

• Primary Device ID: 07350081494872
• NIH Device Record Key: b3fcb02c-cdeb-4010-a6ca-70ec5c97f33a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atlas Surgical and Prosthetic Instrumentation Kit
• Version Model Number: AK-3
• Catalog Number: AK-3
• Company DUNS: 355803412
• Company Name: Dentatus AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +12124811010
• Email: dentatus@dentatus.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350081494872 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[07350081494872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-10

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